Stryker recalls iBur 3.0mm Diamond Match Heads for potential thermal injury during bone procedures. Affected units have specific lot numbers and were sold for neuro, spine, ENT, and endoscopic surgeries.
Potential for the product to exhibit temperatures higher than specification where the bur shank meets the distal bushing. Temperatures higher than specification may lead to the potential for minor tissue/structure damage or tissue/structure damage from thermal injury which may need medical/surgical intervention.
Stryker is recalling certain iBur 3.0mm Diamond Match Heads used in bone surgery due to a risk of overheating at the bur shank. This could cause minor tissue damage or require medical intervention if the device gets too hot during use.
The bur shank can overheat when it meets the distal bushing during bone cutting. This overheating might cause minor tissue damage or require medical attention if the temperature exceeds safe levels.
Surgery professionals using the iBur 3.0mm Diamond Match Heads for bone procedures in neuro, spine, ENT, or endoscopic surgeries. Those with specific lot numbers are most at risk.
Check for lot numbers 22334017, 23047017, 23095017, or 23198017 on the product packaging. These iBurs are used for bone cutting in neuro, spine, ENT, or endoscopic procedures.
Look for lot numbers 22334017, 23047017, 23095017, or 23198017 on the packaging.
The iBur 3.0mm Diamond Match Heads can overheat at the bur shank during bone cutting, potentially causing minor tissue damage or requiring medical intervention.
Check the lot number on the packaging. If it matches the affected numbers (22334017, 23047017, 23095017, 23198017), stop using it and contact Stryker for guidance.
The recall record does not mention a specific fix or remedy for this issue.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2730-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2730-2024 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
